279 related articles for article (PubMed ID: 22043907)
1. Upregulation of micro RNA-146a (miRNA-146a), a marker for inflammatory neurodegeneration, in sporadic Creutzfeldt-Jakob disease (sCJD) and Gerstmann-Straussler-Scheinker (GSS) syndrome.
Lukiw WJ; Dua P; Pogue AI; Eicken C; Hill JM
J Toxicol Environ Health A; 2011; 74(22-24):1460-8. PubMed ID: 22043907
[TBL] [Abstract][Full Text] [Related]
2. microRNA-146a-5p, Neurotropic Viral Infection and Prion Disease (PrD).
Pogue AI; Lukiw WJ
Int J Mol Sci; 2021 Aug; 22(17):. PubMed ID: 34502105
[TBL] [Abstract][Full Text] [Related]
3. Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease.
Sikorska B; Liberski PP; Sobów T; Budka H; Ironside JW
Neuropathol Appl Neurobiol; 2009 Feb; 35(1):46-59. PubMed ID: 18513219
[TBL] [Abstract][Full Text] [Related]
4. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.
Zanusso G; Fiorini M; Ferrari S; Meade-White K; Barbieri I; Brocchi E; Ghetti B; Monaco S
J Biol Chem; 2014 Feb; 289(8):4870-81. PubMed ID: 24398683
[TBL] [Abstract][Full Text] [Related]
5. microRNA-146a as a biomarker for transmissible spongiform encephalopathy.
Pogue A; Zhao Y; Lukiw W
Folia Neuropathol; 2022; 60(1):24-34. PubMed ID: 35359143
[TBL] [Abstract][Full Text] [Related]
6. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.
Di Fede G; Giaccone G; Limido L; Mangieri M; Suardi S; Puoti G; Morbin M; Mazzoleni G; Ghetti B; Tagliavini F
J Neuropathol Exp Neurol; 2007 Feb; 66(2):124-30. PubMed ID: 17278997
[TBL] [Abstract][Full Text] [Related]
7. Characterization of an NF-kappaB-regulated, miRNA-146a-mediated down-regulation of complement factor H (CFH) in metal-sulfate-stressed human brain cells.
Pogue AI; Li YY; Cui JG; Zhao Y; Kruck TP; Percy ME; Tarr MA; Lukiw WJ
J Inorg Biochem; 2009 Nov; 103(11):1591-5. PubMed ID: 19540598
[TBL] [Abstract][Full Text] [Related]
8. Sporadic Creutzfeldt-Jakob Disease in a Woman Married Into a Gerstmann-Sträussler-Scheinker Family: An Investigation of Prions Transmission via Microchimerism.
Areškeviciute A; Melchior LC; Broholm H; Krarup LH; Lindquist SG; Johansen P; McKenzie N; Green A; Nielsen JE; Laursen H; Lund EL
J Neuropathol Exp Neurol; 2018 Aug; 77(8):673-684. PubMed ID: 29889261
[TBL] [Abstract][Full Text] [Related]
9. An NF-kappaB-sensitive micro RNA-146a-mediated inflammatory circuit in Alzheimer disease and in stressed human brain cells.
Lukiw WJ; Zhao Y; Cui JG
J Biol Chem; 2008 Nov; 283(46):31315-22. PubMed ID: 18801740
[TBL] [Abstract][Full Text] [Related]
10. Targeting the cellular prion protein to treat neurodegeneration.
Biasini E; Harris DA
Future Med Chem; 2012 Sep; 4(13):1655-8. PubMed ID: 22924502
[No Abstract] [Full Text] [Related]
11. A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob disease.
Furukawa H; Doh-ura K; Kikuchi H; Tateishi J; Iwaki T
J Neurol Sci; 1998 Jun; 158(1):71-5. PubMed ID: 9667781
[TBL] [Abstract][Full Text] [Related]
12. Towards authentic transgenic mouse models of heritable PrP prion diseases.
Watts JC; Giles K; Bourkas ME; Patel S; Oehler A; Gavidia M; Bhardwaj S; Lee J; Prusiner SB
Acta Neuropathol; 2016 Oct; 132(4):593-610. PubMed ID: 27350609
[TBL] [Abstract][Full Text] [Related]
13. Immunohistochemical localization of 14.3.3 zeta protein in amyloid plaques in human spongiform encephalopathies.
Richard M; Biacabe AG; Streichenberger N; Ironside JW; Mohr M; Kopp N; Perret-Liaudet A
Acta Neuropathol; 2003 Mar; 105(3):296-302. PubMed ID: 12557018
[TBL] [Abstract][Full Text] [Related]
14. Relationship of microglia and scrapie amyloid-immunoreactive plaques in kuru, Creutzfeldt-Jakob disease and Gerstmann-Sträussler syndrome.
Guiroy DC; Wakayama I; Liberski PP; Gajdusek DC
Acta Neuropathol; 1994; 87(5):526-30. PubMed ID: 8059606
[TBL] [Abstract][Full Text] [Related]
15. Silence of resident microglia in GPI anchorless prion disease and activation of microglia in Gerstmann-Sträussler-Scheinker disease and sporadic Creutzfeldt-Jakob disease.
Noguchi H; Koyama S; Yagita K; Shijo M; Matsuzono K; Hamasaki H; Kanemaru T; Okamoto T; Kai K; Aishima S; Abe K; Sasagasako N; Honda H
J Neuropathol Exp Neurol; 2022 Dec; 82(1):38-48. PubMed ID: 36331509
[TBL] [Abstract][Full Text] [Related]
16. Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred).
Piccardo P; Seiler C; Dlouhy SR; Young K; Farlow MR; Prelli F; Frangione B; Bugiani O; Tagliavini F; Ghetti B
J Neuropathol Exp Neurol; 1996 Nov; 55(11):1157-63. PubMed ID: 8939199
[TBL] [Abstract][Full Text] [Related]
17. Creutzfeldt-Jakob disease with Alzheimer-type A beta-reactive amyloid plaques.
Barcikowska M; Kwiecinski H; Liberski PP; Kowalski J; Brown P; Gajdusek DC
Histopathology; 1995 May; 26(5):445-50. PubMed ID: 7657313
[TBL] [Abstract][Full Text] [Related]
18. [Creutzfeldt-Jakob disease(CJD) and Gerstmann-Sträussler-Scheinker syndrome(GSS)].
Udaka F; Fujisawa M; Kameyama M
Nihon Rinsho; 1997 Apr; 55(4):972-7. PubMed ID: 9103904
[TBL] [Abstract][Full Text] [Related]
19. Localization of A11-reactive oligomeric species in prion diseases.
Aidt FH; Hasholt LF; Christiansen M; Laursen H
Histopathology; 2013 Jun; 62(7):994-1001. PubMed ID: 23570304
[TBL] [Abstract][Full Text] [Related]
20. Accumulation of Astrocytic Aquaporin 4 and Aquaporin 1 in Prion Protein Plaques.
Sadashima S; Honda H; Suzuki SO; Shijo M; Aishima S; Kai K; Kira J; Iwaki T
J Neuropathol Exp Neurol; 2020 Apr; 79(4):419-429. PubMed ID: 32167542
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]